Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.3073068A>G , CM000666.2:g.3073068A>G | GRCh38 |
| NC_000004.11:g.3074795A>G , CM000666.1:g.3074795A>G | GRCh37 |
| NC_000004.10:g.3044593A>G | NCBI36 |
| NG_009378.1:g.3388A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_045414.1:n.89+1358T>C (HTT-AS) | |
| ENST00000647962.1:n.1203-290A>G (HTT) | |
| ENST00000649900.1:n.504-13871A>G (HTT) | |
| ENST00000680239.1:c.6-13871A>G (HTT) | ENSP00000506169.1:n.6-13871A>G |
| ENST00000680360.1:c.6-13871A>G (HTT) | ENSP00000505014.1:n.6-13871A>G |
| ENST00000680956.1:c.6-13871A>G (HTT) | ENSP00000506029.1:n.6-13871A>G |
| ENST00000681528.1:c.6-13871A>G (HTT) | ENSP00000506116.1:n.6-13871A>G |